CLC4E Rabbit Polyclonal Antibody, 50ul Cell Culture & Maintenance Mutations or deletions in this

Mutations or deletions in this gene have been shown to result in pancreatic cancer

subcellular location:Nuclear and perinuclear Golgi region

disease:A chromosomal aberration involving NUT is found in a rare

are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA)

CLC4E Rabbit Polyclonal Antibody, 50ul Cell Culture & Maintenance Mutations or deletions in thisThis gene encodes a member of the C type lectin C type lectin like domain (CTL CTLD) superfamily. Members of this family share a common protein fold and have diverse functions such as cell adhesion cell cell signalling glycoprotein turnover and roles in inflammation and immune response. The encoded type II transmembrane protein is a downstream target of CCAAT enhancer binding protein (C EBP) beta (CEBPB) and may play a role in inflammation.